Resistance Training Diminishes the Expression of Exosome CD63 Protein without Modification of Plasma miR-146a-5p and cfDNA in the Elderly

Aging-associated inflammation is characterized by senescent cell-mediated secretion of high levels of inflammatory mediators, such as microRNA (miR)-146a. Moreover, a rise of circulating cell-free DNA (cfDNA) is also related to systemic inflammation and frailty in the elderly. Exosome-mediated cell-...

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Veröffentlicht in:Nutrients 2021-02, Vol.13 (2), p.665
Hauptverfasser: Estébanez, Brisamar, Visavadiya, Nishant P, de Paz, José A, Whitehurst, Michael, Cuevas, María J, González-Gallego, Javier, Huang, Chun-Jung
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container_start_page 665
container_title Nutrients
container_volume 13
creator Estébanez, Brisamar
Visavadiya, Nishant P
de Paz, José A
Whitehurst, Michael
Cuevas, María J
González-Gallego, Javier
Huang, Chun-Jung
description Aging-associated inflammation is characterized by senescent cell-mediated secretion of high levels of inflammatory mediators, such as microRNA (miR)-146a. Moreover, a rise of circulating cell-free DNA (cfDNA) is also related to systemic inflammation and frailty in the elderly. Exosome-mediated cell-to-cell communication is fundamental in cellular senescence and aging. The plasma changes in exercise-promoted miR-146a-5p, cfDNA, and exosome release could be the key to facilitate intercellular communication and systemic adaptations to exercise in aging. Thirty-eight elderly subjects (28 trained and 10 controls) volunteered in an 8-week resistance training protocol. The levels of plasma miR-146a-5p, cfDNA, and exosome markers (CD9, CD14, CD63, CD81, Flotillin [Flot]-1, and VDAC1) were measured prior to and following training. Results showed no changes in plasma miR-146a-5p and cfDNA levels with training. The levels of exosome markers (Flot-1, CD9, and CD81) as well as exosome-carried proteins (CD14 and VDAC1) remained unchanged, whereas an attenuated CD63 response was found in the trained group compared to the controls. These findings might partially support the anti-inflammatory effect of resistance training in the elderly as evidenced by the diminishment of exosome CD63 protein expression, without modification of plasma miR-146a-5p and cfDNA.
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Moreover, a rise of circulating cell-free DNA (cfDNA) is also related to systemic inflammation and frailty in the elderly. Exosome-mediated cell-to-cell communication is fundamental in cellular senescence and aging. The plasma changes in exercise-promoted miR-146a-5p, cfDNA, and exosome release could be the key to facilitate intercellular communication and systemic adaptations to exercise in aging. Thirty-eight elderly subjects (28 trained and 10 controls) volunteered in an 8-week resistance training protocol. The levels of plasma miR-146a-5p, cfDNA, and exosome markers (CD9, CD14, CD63, CD81, Flotillin [Flot]-1, and VDAC1) were measured prior to and following training. Results showed no changes in plasma miR-146a-5p and cfDNA levels with training. The levels of exosome markers (Flot-1, CD9, and CD81) as well as exosome-carried proteins (CD14 and VDAC1) remained unchanged, whereas an attenuated CD63 response was found in the trained group compared to the controls. 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This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). 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Moreover, a rise of circulating cell-free DNA (cfDNA) is also related to systemic inflammation and frailty in the elderly. Exosome-mediated cell-to-cell communication is fundamental in cellular senescence and aging. The plasma changes in exercise-promoted miR-146a-5p, cfDNA, and exosome release could be the key to facilitate intercellular communication and systemic adaptations to exercise in aging. Thirty-eight elderly subjects (28 trained and 10 controls) volunteered in an 8-week resistance training protocol. The levels of plasma miR-146a-5p, cfDNA, and exosome markers (CD9, CD14, CD63, CD81, Flotillin [Flot]-1, and VDAC1) were measured prior to and following training. Results showed no changes in plasma miR-146a-5p and cfDNA levels with training. The levels of exosome markers (Flot-1, CD9, and CD81) as well as exosome-carried proteins (CD14 and VDAC1) remained unchanged, whereas an attenuated CD63 response was found in the trained group compared to the controls. 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subjects Adaptation
Aged
Aged, 80 and over
Aging
Aging - physiology
CD14 antigen
CD63 antigen
CD81 antigen
CD9 antigen
Cell Communication
Cell signaling
Cell-Free Nucleic Acids - blood
Deoxyribonucleic acid
Diabetes
DNA
Ethylenediaminetetraacetic acid
Exercise
Exercise - physiology
Exosomes - chemistry
Exosomes - physiology
Female
Fitness training programs
Gene Expression - physiology
Geriatrics
Humans
Inflammation
Inflammation - prevention & control
Male
Males
Medical screening
MicroRNA
MicroRNAs
MicroRNAs - blood
miRNA
Older people
Physical fitness
Physical training
Plasma
Proteins
Range of motion
Resistance Training
Senescence
Strength training
Tetraspanin 30 - blood
Tetraspanin 30 - genetics
Type 2 diabetes
Weight training
Young Adult
title Resistance Training Diminishes the Expression of Exosome CD63 Protein without Modification of Plasma miR-146a-5p and cfDNA in the Elderly
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